TIMX 202586

GUDID 10705034000596

TIMX LOW BACK SYSTEM HEXLOBE DRIVER

DEPUY SPINE, LLC

Orthopaedic implant driver

• Primary Device ID: 10705034000596
• NIH Device Record Key: a3ccc30d-0182-4f75-b950-5fd2c7929ccc
• Commercial Distribution Discontinuation: 2019-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TIMX
• Version Model Number: 202586
• Catalog Number: 202586
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034000596 [Primary]

FDA Product Code

• HWR: DRIVER, PROSTHESIS

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10705034000596]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-12-12
• Device Publish Date: 2016-12-31

On-Brand Devices [TIMX]

• 10705034008349: TIMX LOW BACK SYSTEM TORQUE WRENCH-SHAFT
• 10705034241463: TIMX LOW BACK SYSTEM HEXLOBE SET SCREW M6 9.30mm
• 10705034000596: TIMX LOW BACK SYSTEM HEXLOBE DRIVER
• 10705034241470: TIMX LOW BACK SYSTEM SET SCREW-METRIC THREAD M7 9.30mm